2-Methylbutyryl-Co A Dehydrogenase Deficiency

2-Methylbutyryl-Co A Dehydrogenase Deficiency

2-Methylbutyryl-CoA dehydrogenase deficiency, also called 2-Methylbutyryl glycinuria or short/branched-chain acyl-CoA dehydrogenase deficiency (SBCADD), is an autosomal recessive metabolic disorder. It causes the body to be unable to process the amino acid isoleucine properly.

Read more about 2-Methylbutyryl-Co A Dehydrogenase Deficiency:  Signs and Symptoms, Cause and Genetics

Famous quotes containing the word deficiency:

    All rejection and negation indicates a deficiency in fertility: fundamentally, if only we were good plowland we would allow nothing to go unused, and in every thing, event, and person we would welcome manure, rain, or sunshine.
    Friedrich Nietzsche (1844–1900)